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衰老相关的窖蛋白-1 表达增加促进神经元中 α-突触核蛋白的细胞间传递。

Age-related increase in caveolin-1 expression facilitates cell-to-cell transmission of α-synuclein in neurons.

机构信息

Department of Pharmacology, Ajou University School of Medicine, 164, Worldcup-ro, Yeongtong-gu, Suwon, 16499, Korea.

Center for Convergence Research of Neurological Disorders, Ajou University School of Medicine, Suwon, Korea.

出版信息

Mol Brain. 2021 Jul 28;14(1):122. doi: 10.1186/s13041-021-00834-2.

Abstract

Parkinson's disease (PD) is the second most prevalent neurodegenerative disease, with aging being considered the greatest risk factor for developing PD. Caveolin-1 (Cav-1) is known to participate in the aging process. Recent evidence indicates that prion-like propagation of misfolded α-synuclein (α-syn) released from neurons to neighboring neurons plays an important role in PD progression. In the present study, we demonstrated that cav-1 expression in the brain increased with age, and considerably increased in the brain of A53T α-syn transgenic mice. Cav-1 overexpression facilitated the uptake of α-syn into neurons and formation of additional Lewy body-like inclusion bodies, phosphorylation of cav-1 at tyrosine 14 was found to be crucial for this process. This study demonstrates the relationship between age and α-syn spread and will facilitate our understanding of the molecular mechanism of the cell-to-cell transmission of α-syn.

摘要

帕金森病(PD)是第二大常见的神经退行性疾病,衰老被认为是发生 PD 的最大风险因素。小窝蛋白-1(Cav-1)已知参与衰老过程。最近的证据表明,从神经元释放的错误折叠的α-突触核蛋白(α-syn)的类朊病毒样传播在 PD 进展中起着重要作用。在本研究中,我们证明了大脑中 cav-1 的表达随年龄增长而增加,并且在 A53T α-syn 转基因小鼠的大脑中显著增加。Cav-1 过表达促进了 α-syn 进入神经元并形成额外的路易体样包涵体,发现酪氨酸 14 上的 cav-1 磷酸化对于该过程至关重要。这项研究表明了年龄与 α-syn 传播之间的关系,并将有助于我们理解 α-syn 细胞间传递的分子机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3973/8320051/1d2580313fb2/13041_2021_834_Fig1_HTML.jpg

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